is potentially life threatening (Pneumonia‚ Severe Exacerbation of Chronic obstructive pulmonary disorder (COPD)‚ Pulmonary embolism (PE)‚ or Heart Failure) or not (Upper respiratory infection (URI)‚ Lower respiratory infection (LRI)‚ Asthma‚ Bronchiectasis‚ Upper Airway Cough Syndrome (UACS)‚ and COPD). Pratter et al. (2006) found that in managing patients with subacute cough the first step is to determine whether or not the cough has followed an obvious preceding respiratory infection. According
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This may lead to changes within the body similar to bronchiectasis. As a matter of fact‚ “Kartegener’s syndrome accounts for as much as 20% of all congenital bronchiectasis (Clinical Manifestations).” These Anatomical Alterations include increased bronchial wall thickness due to scar tissue‚ hyperinflation of the lungs and an increased size of the airways. Common symptoms associated with bronchiectasis include a chronic cough‚ fatigue‚ and increased work of breathing. The diagnosis
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Cystic fibrosis is when thick mucus is produced due to a hereditary genetic disorder; the mucus produced is so thick that it clogs the body’s tubes and passageways. Cystic fibrosis is caused by the mutation in a gene known as the CFTR gene; this fault in the gene causes the normal workings of a protein to be blocked allowing too much salt and not enough water into cells. These result in the build-up of thick mucus in the body’s tubes and passageways blocking them‚ these blockages damage the lungs
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famous for his experiment with the kite and key. Rene Laennec invented the Stethoscope. With this he investigated sounds made by the heart and lungs‚ and compared it to his diagnosis he got from autopsies. He also wrote the first descriptions of bronchiectasis and cirrhosis and also classified lung conditions like pneumonia‚ pleurisy and emphysema. Lastly‚ John Hunter was a surgeon of the 18th century and is now known as founder of “scientific surgery.” He made many advances in surgical procedures
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Research Article 2: Questions “Cilia and Diseases” 1. Where are cilia found in the human body and what do they do? (2 points) Cilia can be found in the human body located inside almost each cell. Cilia inside the brain serve the function of circulating cerebrospinal fluid. The cilia in the repertory system move particle matter and mucus out of the lungs. 2. Describe the structure of a normal cilia? (3 points) Normal cilia are hair like‚ that extend from the body of a cell into the extracellular
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the following tests done except ____________. arterial blood gas test Question The combining form that means lung or air is: pneum/o. Question Chronic‚ permanent enlargement and loss of flexibility of the bronchioles is bronchiectasis. Question Pneumonia is . an infection of some or all of the lobes of the lung. Question Anoxia refers to the lack of __________________________‚ whereas hypercapnia refers to an abnormally high level of __________________________
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During the physical examination‚ we were unable to elicit findings typical of pneumonia such as dullness on both the lower lung fields‚ crackles‚ and increased breath sounds. We attributed this to the medications that were already taking effect on the day prior to conducting the physical examination. Administration of antibiotics and expectorants relieves the pulmonary congestion by reducing the bacterial load and purging the mucus that clogs the bronchi. The resolution of the disease in the patient
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adenoid/o adenoids Adenoidectomy adenoid hypertrophy alveol/o alveolus‚ air sac alveolar bronch/o bronchi/o bronchial tube‚ bronchus Bronchospasm: This tightening of the bronchus is a chief characteristic of asthma and bronchitis Bronchiectasis: Caused by weakening of the bronchial wall from infection. Bronchodilator: This drug causes dilation‚ or enlargement‚ of the opening of a bronchus to improve ventilation to the lungs. An example is albuterol‚ delivered via an inhaler. Bronchopleural:
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poor weight gain and greasy stools can be a sign of CF. If a child ever has any of these symptoms‚ they should seek medical attention as soon as possible. Cystic Fibrosis can lead to many respiratory complications such as: a collapsed lung‚ bronchiectasis‚ chronic infections‚ nasal polyps‚ and can eventually lead to respiratory
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Copyright #ERS Journals Ltd 2002 European Respiratory Journal ISSN 0903-1936 Eur Respir J 2002; 19: 6–7 DOI: 10.1183/09031936.02.00281002 Printed in UK – all rights reserved EDITORIAL Understanding cough A.H. Morice*‚ J. Widdicombe#‚ P. Dicpinigaitis}‚ L. Groenkez A recent meeting on antitussive strategies presented an opportunity to review current practice in the treatment of acute cough due to respiratory tract infection (RTI). Multiple factors contribute to the present lack
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